AEG 3482 - ≥99%(HPLC) , CAS No.63735-71-7

CAS: 63735-71-7 Cat. No.: A287091 Formula: C₁₀H₈N₄O₂S₂ Peso molecolare: 280.33

GRADE & PURITY ≥99%(HPLC)

Synonyms

6-phenylimidazo[2,1-b][1,3,4]thiadiazole-2-sulfonamide | NCGC00167812-02 | Q27195229 | NCGC00167812-06 | Oprea1_698164 | SCHEMBL2540289 | 7EZF1A283N | HMS3677N15 | BCP01890 | CCG-221955 | NCGC00167812-01 | HY-107599 | AEG3482 | AEG-3482 | HMS1538B12 | Imi

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Specifications

Sinonimi

6-phenylimidazo[2,1-b][1,3,4]thiadiazole-2-sulfonamide | NCGC00167812-02 | Q27195229 | NCGC00167812-06 | Oprea1_698164 | SCHEMBL2540289 | 7EZF1A283N | HMS3677N15 | BCP01890 | CCG-221955 | NCGC00167812-01 | HY-107599 | AEG3482 | AEG-3482 | HMS1538B12 | Imi

Specifiche e purezza

≥99%(HPLC)

Meccanismi biochimici e fisiologici

Inhibitor of c-jun N-terminal kinase (JNK) signaling. Binds Hsp90 and facilitates HSF1 release, induces expression of Hsp70, which in turn blocks JNK activation and JNK-dependent apoptosis. Antiapoptotic; inhibits NGF withdrawal-induced death in SCG neuro

Condizioni di conservazione di stoccaggio

Store at -20°C

Spedito in

Ice chest + Ice pads

Questo prodotto richiede spedizione a catena fredda. I servizi di terra e altri servizi economici non sono disponibili.

Tipo di azione

INHIBITOR

Purezza

≥99%(HPLC)

Nomi e identificatori

• Pubchem Sid: 528763033
• Sorrisi canonici: C1=CC=C(C=C1)C2=CN3C(=N2)SC(=N3)S(=O)(=O)N
• IUPAC Name: 6-phenylimidazo[2,1-b][1,3,4]thiadiazole-2-sulfonamide
• InChIKey: MQUYTXDAVCOCMX-UHFFFAOYSA-N
• INCHI: 1S/C10H8N4O2S2/c11-18(15,16)10-13-14-6-8(12-9(14)17-10)7-4-2-1-3-5-7/h1-6H,(H2,11,15,16)
• Isomeri SMILES: C1=CC=C(C=C1)C2=CN3C(=N2)SC(=N3)S(=O)(=O)N
• WGK Germania: 3
• Peso molecolare: 280.33
• Reaxy-Rn: 1007641
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1007641&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Classe Azoles
      • Subclass Imidazoles
        • Level5 Substituted imidazoles
          • Level6 Phenylimidazoles

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Classe: Azoles
• Subclass: Imidazoles
• Intermediate Tree Nodes: Substituted imidazoles
• Direct Parent: Phenylimidazoles
• Alternative Parents: Thiadiazole sulfonamides Organosulfonamides N-substituted imidazoles Benzene and substituted derivatives Heteroaromatic compounds Aminosulfonyl compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic heteropolycyclic compounds
• Substituents: 5-phenylimidazole - 4-phenylimidazole - 1,3,4-thiadiazole-2-sulfonamide - Monocyclic benzene moiety - N-substituted imidazole - Organosulfonic acid amide - Benzenoid - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Heteroaromatic compound - Sulfonyl - Thiadiazole - Aminosulfonyl compound - Azacycle - Organic oxide - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organosulfur compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as phenylimidazoles. These are polycyclic aromatic compounds containing a benzene ring linked to an imidazole ring through a CC or CN bond.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Obiettivi associati (umani)

MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)

Discover Target: MEN1

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Obiettivi associati (non umani)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

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Mus musculus (284745 Activities)

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rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

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Rorc Nuclear receptor ROR-gamma (89407 Activities)

Discover Target: Rorc

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Meccanismi d'azione

Proprietà chimiche e fisiche

• Solubilità: Solvent:DMSO, Max Conc. mg/mL: 28.03, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 1.4, Max Conc. mM: 5
• Peso molecolare: 280.300 g/mol
• XLogP3: 1.400
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 280.009 Da
• Monoisotopic Mass: 280.009 Da
• Topological Polar Surface Area: 127.000 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 405.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1